Juvenile Idiopathic Arthritis, Uveitis and Multiple Sclerosis: Description of Two Patients and Literature Review.

anti-TNF-α agents comorbidity juvenile idiopathic arthritis multiple sclerosis treatment

Journal

Biomedicines
ISSN: 2227-9059
Titre abrégé: Biomedicines
Pays: Switzerland
ID NLM: 101691304

Informations de publication

Date de publication:
21 Aug 2022
Historique:
received: 26 07 2022
revised: 16 08 2022
accepted: 17 08 2022
entrez: 26 8 2022
pubmed: 27 8 2022
medline: 27 8 2022
Statut: epublish

Résumé

Juvenile idiopathic arthritis (JIA) is the most common rheumatic disease in childhood, while multiple sclerosis (MS) is a demyelinating disease of the central nervous system, characterized by remission and exacerbation phases. An association between MS and rheumatologic diseases, in particular rheumatoid arthritis, has been described and numerous studies acknowledge anti-TNF-α drugs as MS triggers. Conversely, the association between MS and JIA has been reported merely in five cases in the literature. We describe two cases of adult patients with longstanding JIA and JIA-associated uveitis, who developed MS. The first patient was on methotrexate and adalimumab when she developed dizziness and nausea. Characteristic MRI lesions and oligoclonal bands in cerebrospinal fluid led to MS diagnosis. Adalimumab was discontinued, and she was treated with three pulses of intravenous methylprednisolone. After a few months, rituximab was started. The second patient had been treated with anti-TNF-α and then switched to abatacept. She complained of unilateral arm and facial paraesthesias; brain MRI showed characteristic lesions, and MS was diagnosed. Three pulses of intravenous methylprednisolone were administered; neurological disease remained stable, and abatacept was reintroduced. Further studies are warranted to define if there is an association between JIA and MS, if MS represents JIA comorbidity or if anti-TNF-α underpins MS development.

Identifiants

pubmed: 36009588
pii: biomedicines10082041
doi: 10.3390/biomedicines10082041
pmc: PMC9405697
pii:
doi:

Types de publication

Case Reports

Langues

eng

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Auteurs

Cecilia Beatrice Chighizola (CB)

Department of Clinical Sciences and Community Health, University of Milan, 20122 Milan, Italy.
Paediatric Rheumatology Unit, ASST G. Pini & CTO, 20122 Milan, Italy.

Matteo Ferrito (M)

Department of Clinical Sciences and Community Health, University of Milan, 20122 Milan, Italy.
Clinical Rheumatology Unit, ASST G. Pini & CTO, 20122 Milan, Italy.

Luca Marelli (L)

Department of Clinical Sciences and Community Health, University of Milan, 20122 Milan, Italy.
Eye Clinic, San Giuseppe Hospital, IRCCS Multimedica, 20123 Milan, Italy.

Irene Pontikaki (I)

Paediatric Rheumatology Unit, ASST G. Pini & CTO, 20122 Milan, Italy.

Paolo Nucci (P)

Eye Clinic, San Giuseppe Hospital, IRCCS Multimedica, 20123 Milan, Italy.
Department of Biomedical, Surgical and Dental Sciences, University of Milan, 20122 Milan, Italy.

Elisabetta Miserocchi (E)

Uveitis Service, IRCCS Ospedale San Raffaele, Università Vita-Salute, Via Olgettina 60, 20132 Milan, Italy.

Roberto Caporali (R)

Department of Clinical Sciences and Community Health, University of Milan, 20122 Milan, Italy.
Clinical Rheumatology Unit, ASST G. Pini & CTO, 20122 Milan, Italy.

Classifications MeSH